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LCS COMPLETE 1294-09-820Recalls & reported problems

Depuy Orthopaedics, Inc. · LCS COMPLETE 3 Peg Patella Metal Backed Poly Replacement SML+ · Class 3 · Implant

All models of LCS COMPLETE (117)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295022763), received between Sep 25, 2020 and Sep 25, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Naturally Worn” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Naturally Worn1

Patient problems

  • No Code Available1
  • Pain1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 25, 2020Naturally Worn; Naturally Worn

    THE PATIENT WAS REVISED TO ADDRESS PAIN DUE TO WORN POLY. ORIGINAL IMPLANT DATE IS UNKNOWN. DOI: UNKNOWN, DOR: (B)(6) 2020, LEFT KNEE.

    Patient problems: No Code Available; Pain

    MAUDE report 10587525 ↗

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Sources and updates

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